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¾ÆÁñ·ÎÁÖ1g(¾ÆÁñ·Î½Ç¸°³ªÆ®·ý) AZLO INJ.[Azlocillin Sodium]
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µå·°ÀÎÆ÷¿¡¼´Â ÀǾàǰ ÀÎÅÍ³Ý ÆÇ¸Å¸¦ ÇÏÁö ¾Ê½À´Ï´Ù. |
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665501800[A14601141]
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\0 ¿ø/1g/º´(2007.03.01)(ÇöÀç¾à°¡)
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112801BIJ
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1¼¼¢¦14¼¼ : 3 x 75mg/Kg/day
7ÀÏ¢¦1¼¼ : 3 x 100mg/Kg/day
7ÀϹ̸¸ : 2x 100mg/Kg/day
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| Related FDA Approved Drug |
±âÁØ ¼ººÐ: AZLOCILLIN SODIUMAZLIN (AZLOCILLIN SODIUM)
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µå·°ÀÎÆ÷ ÀǾàǰ ¿ä¾à/»ó¼¼Á¤º¸
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665501800[A14601141]
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| º¸°ü¹æ¹ý |
Â÷±¤ÇÑ ¹ÐºÀ¿ë±â |
| Brandname Á¤º¸ |
Azlocillin Sodium
Brand Names/Synonyms
- Azlin
- Azlocilina [INN-Spanish]
- Azlocillin sodium salt
- Azlocilline [INN-French]
- Azlocillinum [INN-Latin]
- Bayer Brand of Azlocillin
- Securopen
Brand Name MixturesNot Available
Chemical IUPAC Name3,3-dimethyl-6-oxo-7-[2-(2-oxoimidazolidin-1-yl)carbonylamino-2-phenyl-acetyl]amino- 2-thia-5-azabicyclo[3.2.0]heptane-4-carboxylic acid
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| Mechanism of Action |
Azlocillin¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ By binding to specific penicillin-binding proteins (PBPs) located inside the bacterial cell wall, azlocillin inhibits the third and last stage of bacterial cell wall synthesis. Cell lysis is then mediated by bacterial cell wall autolytic enzymes such as autolysins; it is possible that azlocillin interferes with an autolysin inhibitor.
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| Pharmacology |
Azlocillin¿¡ ´ëÇÑ Pharmacology Á¤º¸ Azlocillin, similar to mezlocillin and piperacillin, is an acylampicillin with an extended spectrum of activity and greater in vitro potency than the carboxy penicillins. Azlocillin demonstrates antibacterial activity against a broad spectrum of bacteria, including Pseudomonas aeruginosa, and, in contrast to most cephalosporins, exhibits activity against enterococci.
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| Metabolism |
Azlocillin¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Not Available
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| Protein Binding |
Azlocillin¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 20 to 46% bound to plasma proteins
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| Half-life |
Azlocillin¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ Mean elimination half-life is 1.3 to 1.5 hours. Longer in neonates, and 2 to 6 hours in patients with renal impairment.
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| Absorption |
Azlocillin¿¡ ´ëÇÑ Absorption Á¤º¸ Not significantly absorbed from the gastrointestinal tract.
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| Biotransformation |
Azlocillin¿¡ ´ëÇÑ Biotransformation Á¤º¸ Eliminated predominantly by renal mechanisms, but also undergoes biotransformation within body tissues and intraintestinal degradation by bowel bacteria, with high concentrations found in bile.
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| Toxicity |
Azlocillin¿¡ ´ëÇÑ Toxicity Á¤º¸ Not Available
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| Drug Interactions |
Azlocillin¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Methotrexate The penicillin increases the effect and toxicity of methotrexateDemeclocycline Possible antagonism of actionDoxycycline Possible antagonism of actionEthinyl Estradiol This anti-infectious agent could decrease the effect of the oral contraceptiveMethacycline Possible antagonism of actionMinocycline Possible antagonism of actionOxytetracycline Possible antagonism of actionRolitetracycline Possible antagonism of actionTetracycline Possible antagonism of actionMestranol This anti-infectious agent could decrease the effect of the oral contraceptive
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Azlocillin¿¡ ´ëÇÑ Food Interaction Á¤º¸ Not Available
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| Description |
Azlocillin¿¡ ´ëÇÑ Description Á¤º¸ A semisynthetic ampicillin-derived acylureido penicillin. [PubChem]
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| Dosage Form |
Azlocillin¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Not Available
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| Smiles String Canonical |
Azlocillin¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC1(C)SC2C(NC(=O)C(NC(=O)N3CCNC3=O)C3=CC=CC=C3)C(=O)N2C1C(O)=O
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| Smiles String Isomeric |
Azlocillin¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CC1(C)S[C@@H]2[C@H](NC(=O)[C@H](NC(=O)N3CCNC3=O)C3=CC=CC=C3)C(=O)N2[C@H]1C(O)=O
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| InChI Identifier |
Azlocillin¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C20H23N5O6S/c1-20(2)13(17(28)29)25-15(27)12(16(25)32-20)22-14(26)11(10-6-4-3-5-7-10)23-19(31)24-9-8-21-18(24)30/h3-7,11-13,16H,8-9H2,1-2H3,(H,21,30)(H,22,26)(H,23,31)(H,28,29)/t11?,12-,13+,16-/m1/s1/f/h21-23,28H
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| Chemical IUPAC Name |
Azlocillin¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (2S,5R,6R)-3,3-dimethyl-7-oxo-6-[[2-[(2-oxoimidazolidine-1-carbonyl)amino]-2-phenylacetyl]amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
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